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String and Ball-Like TiO_2/rGO Composites with High Photo-catalysis Degradation Capability for Methylene Blue 被引量:1
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作者 Fengyun Xu Ping Na 《Transactions of Tianjin University》 EI CAS 2018年第3期272-281,共10页
Novelthree-dimensionalstring and ball-like titanium dioxide/reduced graphene oxide, TiO_2/rGO(STG) composites were prepared using a one-step hydrolysis process followed by a low-temperature hydrothermaltreatment. The ... Novelthree-dimensionalstring and ball-like titanium dioxide/reduced graphene oxide, TiO_2/rGO(STG) composites were prepared using a one-step hydrolysis process followed by a low-temperature hydrothermaltreatment. The STG composites exhibited excellent photo-catalytic degradation performance for methylene blue owing to a good synergistic effect between TiO_2 and rGO. The STG composites with 1.0 wt% of rGO loading exhibited the highest removalrate of 86.0% for methylene blue and its reaction rate constant(5.27 × 10^(-3) min^(-1)) was much higher than those of pure string and ball-like TiO_2(ST). In addition, the STG composites also showed an outstanding capability for the photo-catalysis degradation of other cationic dyes. In addition, a possible photo-catalytic degradation mechanism for the STG composite was postulated, in which~?O_2^- and~·OH were the main oxidizing groups. This work of fers new insights into a better design and preparation of novelcomposite materials for the removalof organic dyes. 展开更多
关键词 String and ball-like TiO2 Reduced graphene oxide Synergistic effect Photo-catalytic Methylene blue
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湘西北菱锌矿床地质特征及形成机制 被引量:10
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作者 鲍珏敏 万榕江 包正相 《湖北地矿》 2003年第2期8-12,共5页
湖南西北部龙山 -桑植铅锌矿带的菱锌矿床 ,主要赋存于寒武系上统耗子沱群第 3段和奥陶系下统南津关组底部的“硅化体”与纯灰岩接触面附近 ,为以菱锌矿为主、异极矿其次的氧化锌矿床。矿体呈似层状、透镜状、似脉状等 ,主要产于硅化体... 湖南西北部龙山 -桑植铅锌矿带的菱锌矿床 ,主要赋存于寒武系上统耗子沱群第 3段和奥陶系下统南津关组底部的“硅化体”与纯灰岩接触面附近 ,为以菱锌矿为主、异极矿其次的氧化锌矿床。矿体呈似层状、透镜状、似脉状等 ,主要产于硅化体下部或其沿倾斜延伸位及其尖灭处。具原地或准原地堆积 (主要 )和异地迁移 (次要 )特征。地下水通过层间裂隙、断裂裂隙渗入矿化层及围岩 ,在溶蚀、氧化 -水解作用下形成的菱锌矿床 ,属古岩溶型矿床类型。 展开更多
关键词 湖南 铅锌矿 菱锌矿床 赋存 氧化-水解作用 地下水 层间裂隙 断裂裂隙 形成机制
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Hydrolysis of Aluminum Ions in Kaolinite and Oxisol Suspensions as Influenced by Organic Anions
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作者 XU Ren-Kou XIAO Shuang-Cheng +2 位作者 LI Jiu-Yu D. TIWARI JI Guo-Liang 《Pedosphere》 SCIE CAS CSCD 2007年第1期90-96,共7页
To evaluate the role of kaolinite and variable charge soils on the hydrolytic reaction of Al, the hydrolysis of Al ions in suspensions of a kaolinite and an Oxisol influenced by organic anions was investigated using c... To evaluate the role of kaolinite and variable charge soils on the hydrolytic reaction of Al, the hydrolysis of Al ions in suspensions of a kaolinite and an Oxisol influenced by organic anions was investigated using changes of pH, Al adsorption, and desorption of pre-adsorbed Al. Kaolinite and the Oxisol promoted the hydrolytic reaction of Al above a certain initial Al concentration (0.1 mmol L-1 for kaolinite and 0.3 mmol L-1 for the Oxisol). The Al hydrolysis accelerated by kaolinite and the Oxisol increased with an increase in initial concentration of Al and was observed in the range of pH from 3.7 to 4.7 for kaolinite and 3.9 to 4.9 for the Oxisol. The acceleration of Al hydrolysis also increased with the increase of solution pH, reached a maximum value at pH 4.5, and then decreased sharply. Al hydrolysis was promoted mainly through selective adsorption for hydroxy-Al. Soil free iron oxides compensated a portion of the soil negative charge or masked some soil surface negative sites leading to a decrease in Al adsorption, which retarded acceleration to some extent. For the Oxisol organic anions increased the proportion of adsorbed Al3+ in total adsorbed Al with the increase in soil negative surface charge and eliminated or reduced the acceleration of Al hydrolysis. Different organic anions inhibited the hydrolysis of Al in the order: citrate > oxalate > acetate (under initial pH of 4.5). The formation of Al-organic complexes in solution also inhibited the hydrolysis of Al. 展开更多
关键词 aluminum hydrolysis KAOLINITE organic anion OXISOL
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